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Details

Stereochemistry RACEMIC
Molecular Formula C16H14Cl2O4
Molecular Weight 341.186
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DICLOFOP-METHYL

SMILES

COC(=O)C(C)OC1=CC=C(OC2=C(Cl)C=C(Cl)C=C2)C=C1

InChI

InChIKey=BACHBFVBHLGWSL-UHFFFAOYSA-N
InChI=1S/C16H14Cl2O4/c1-10(16(19)20-2)21-12-4-6-13(7-5-12)22-15-8-3-11(17)9-14(15)18/h3-10H,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative efficacy of five herbicides on winter cereal weeds in semi-arid region of Algeria.
2001
Studies of early hepatocellular proliferation and peroxisomal proliferation in Wistar rats treated with herbicide diclofop.
2001 Feb 14
Resistance to ACCase-inhibiting herbicides and isoproturon in UK populations of Lolium multiflorum: mechanisms of resistance and implications for control.
2001 Jul
Effect of cropping cycles and repeated herbicide applications on the degradation of diclofop-methyl, bentazone, diuron, isoproturon and pendimethalin in soil.
2002 Mar
Tank-mix adjuvants and pesticide residues: some regulatory and quantitative aspects.
2003 Nov
Determination of commonly used herbicides in surface water using solid-phase extraction and dual-column HPLC-DAD.
2005
Recurrent selection with reduced herbicide rates results in the rapid evolution of herbicide resistance in Lolium rigidum.
2005 Apr
Lolium rigidum, a pool of resistance mechanisms to ACCase inhibitor herbicides.
2005 Mar 23
In vitro screening of 200 pesticides for agonistic activity via mouse peroxisome proliferator-activated receptor (PPAR)alpha and PPARgamma and quantitative analysis of in vivo induction pathway.
2006 Dec 15
Enantiomeric resolution of chiral pesticides by high-performance liquid chromatography.
2006 Mar 8
Chiral separations of pesticide enantiomers by high-performance liquid chromatography using cellulose triphenylcarbamate chiral stationary phase.
2006 Nov-Dec
PPARalpha- and DEHP-Induced Cancers.
2008
One- and two-dimensional direct chiral liquid chromatographic determination of mixtures of diclofop-Acid and diclofop-methyl herbicides.
2008 Apr 9
TiO(2)/BaTiO(3)-assisted photocatalytic mineralization of diclofop-methyl on UV-light irradiation in the presence of oxidizing agents.
2009 Mar 15
Environmental behavior of the chiral aryloxyphenoxypropionate herbicide diclofop-methyl and diclofop: enantiomerization and enantioselective degradation in soil.
2010 Mar 15
Impact of environmental chemicals on key transcription regulators and correlation to toxicity end points within EPA's ToxCast program.
2010 Mar 15
Patents
Name Type Language
DICLOFOP-METHYL
ISO   MI  
Common Name English
AVENOXAN
Brand Name English
DICHLORFOP-METHYL
HSDB  
Common Name English
DICHLORFOP-METHYL [HSDB]
Common Name English
PROPANOIC ACID, 2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)-, METHYL ESTER
Systematic Name English
ILLOXAN
Common Name English
HOELON
Common Name English
METHYL DICLOFOP
Common Name English
2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)PROPANOIC ACID, METHYL ESTER
Systematic Name English
DICLOFOP-METHYL [ISO]
Common Name English
HOEGRASS
Common Name English
METHYL 2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)PROPANOATE
Systematic Name English
DICHLORDIPHENPROP
Common Name English
METHYL 2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)PROPIONATE
Systematic Name English
METHYLDICLOFOP
Common Name English
DICLOFOP-METHYL [MI]
Common Name English
DICLOFOP-METHYL, (±)-
Systematic Name English
DICLOFOP METHYL
Common Name English
DICLOFOP METHYL ESTER
Common Name English
DICLOSAN
Common Name English
METHYL 2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)PROPIONATE, (±)-
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 110902
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
Code System Code Type Description
ALANWOOD
diclofop-methyl
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
HSDB
6607
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
FDA UNII
9T8QCB25UO
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
CAS
51338-27-3
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
MERCK INDEX
m4362
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB13918
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
ECHA (EC/EINECS)
257-141-8
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
CHEBI
4510
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID0032605
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
PUBCHEM
39985
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY